| Human Disease |
Smith-Magenis Syndrome; SMS OMIM ID: 182290 |
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| View all models | View ALL (4) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Rai1tm1Jrl/Rai1+ |
B6.129S7-Rai1tm1Jrl/J | J:164451 | View |
| Rai1tm1Jrl/Rai1+ |
involves: 129S/SvEvBrd * C57BL/6 | J:98073 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Del(11Cops3-Gid4)2Jrl/+ |
involves: 129S7/SvEvBrd * C57BL/6 | J:94405 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Del(11Cops3-Rnf112)1Jrl/+ |
involves: 129S7/SvEvBrd * C57BL/6 | J:83302 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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